Abstract
N-Nitrosodialkylamines underwent photolysis in the presence of an acid. From the analysis of the end products, the primary photolysis products were shown to be [NOH] and the corresponding alkylideneimine, which underwent further reaction, e.g. (i) recombination of the two species to give amidoximes, (ii) hyponitrous acid formation, and (iii) hydrolysis or polymerization. A pathway is proposed for the reaction. Evidence is presented to show that the formation of the parent amines was not the result of hydrolysis of nitrosamines.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a callDisclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.
